D3292
2,6-Di-tert-butylphenol
~99% (GC)
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About This Item
Linear Formula:
[(CH3)3C]2C6H3OH
CAS Number:
Molecular Weight:
206.32
EC Number:
204-884-0
UNSPSC Code:
12352200
MDL number:
Beilstein/REAXYS Number:
1841887
InChI key
DKCPKDPYUFEZCP-UHFFFAOYSA-N
InChI
1S/C14H22O/c1-13(2,3)10-8-7-9-11(12(10)15)14(4,5)6/h7-9,15H,1-6H3
SMILES string
CC(C)(C)c1cccc(c1O)C(C)(C)C
vapor pressure
<0.01 mmHg ( 20 °C)
assay
~99% (GC)
bp
253 °C (lit.)
mp
34-37 °C (lit.)
storage temp.
2-8°C
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signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
227.3 °F - closed cup
flash_point_c
108.5 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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G Haeseler et al.
European journal of anaesthesiology, 20(3), 220-224 (2003-03-26)
Propofol is a phenol derivative (2,6 di-isopropylphenol) with a unique effect profile including activating effects on GABA(A) and blocking effects on voltage-operated sodium channels. If the substituents in the 2- and the 6-positions are replaced by tert-butyl groups, the resulting
Mehmet Tümer et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 70(3), 477-481 (2007-09-07)
Crystals of the 3,3'-5,5'-tetra-tert-butyl-4,4'-diphenoquinone (TTBDQ) in the reaction mixture DCM/MeOH (1:1, v/v) were obtained as a result of CC coupling reaction of the sterically hindered phenol (2,6-di-tert-butylphenol, DTBP) using the binuclear Co(II) complexes. The oxidation product (TTBDQ), C(28)H(40)O(2), crystallizes in
Stanley J Stachelek et al.
Journal of biomedical materials research. Part A, 82(4), 1004-1011 (2007-03-21)
Polyurethane cardiovascular implants are subject to oxidation initiated surface degradation, which is mediated by monocyte-derived macrophages (MDM); this often leads to surface cracking and device failure. The present studies examined the hypothesis that covalently attaching antioxidant, di-tert-butylphenol (DBP), to the
A W Girotti et al.
Lipids, 22(6), 401-408 (1987-06-01)
The effects of singlet oxygen- and oxygen radical-induced lipid peroxidation on cell membrane integrity were compared, using the human erythrocyte ghost as a model system. Resealed ghosts underwent lipid peroxidation and lysis (release of trapped glucose-6-P) when irradiated in the
Studies on the synthesis and anti-inflammatory activity of 2,6-di-tert-butylphenols with a heterocyclic group at the 4-position. V. Elimination reaction of the sulfinyl group of 2,3-dihydroimidazo[2,1-b]thiazole 1-oxide.
Y Isomura et al.
Chemical & pharmaceutical bulletin, 32(12), 4726-4730 (1984-12-01)
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